Oligoclonal B-cell leukemia characterized by spontaneous cell division and telomere association

Genes Chromosomes Cancer. 1993 Sep;8(1):49-59. doi: 10.1002/gcc.2870080109.

Abstract

Cytogenetic analysis of unstimulated cultures from a female patient with chronic B-cell leukemia (CLL) revealed three cytogenetically distinct clones, suggesting that the patient's leukemia was oligoclonal. Immunoglobulin heavy chain gene rearrangement studies revealed 1 germline and 4 rearranged bands, indicative of an oligoclonal leukemic population. Further evidence of oligoclonality was provided by X-linked RFLP studies. This is the first report of oligoclonality in CLL demonstrated by cytogenetic, immunoglobulin gene rearrangement, and X-chromosome inactivation studies. In addition to oligoclonality, the patient's leukemic cells exhibited telomere association, a Robertsonian translocation, and clonal evolution, suggesting an underlying genomic instability.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Division
  • Cells, Cultured
  • Chromosomes, Human, Pair 15
  • Female
  • Gene Rearrangement
  • Genes, Immunoglobulin
  • Humans
  • Karyotyping
  • Leukemia, Lymphocytic, Chronic, B-Cell / blood
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics*
  • Leukemia, Lymphocytic, Chronic, B-Cell / immunology
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology
  • Lymphocyte Activation
  • Lymphocytes / immunology
  • Lymphocytes / pathology
  • Middle Aged
  • Polymorphism, Restriction Fragment Length
  • Sex Chromosome Aberrations
  • Telomere / ultrastructure*
  • Translocation, Genetic
  • X Chromosome